Showing posts with label macromolecular. Show all posts
Showing posts with label macromolecular. Show all posts

Thursday, November 7, 2013

Programmed nanoparticles organize themselves into highly complex nanostructures



The self-assembly process described in Nature commences
with chain-like macromolecules, so-called
triblock terpolymers composed of three linear sections
connected to form a chain-like structure
A-B-C or A-D-C. The block in the
middle has been marked green or black,
respectively. Block A (gray) has to interact
with other particles; block C (rose) is a
corona controlling solubility. By way
of self-aggregation the macromolecules
formed nanoparticles, which by way of
co-aggregation formed the next higher
level in the hierarchy. This way a co-assembled
superstructure develops, for which Müller's
research team has coined the term "caterpillar micelles."
©: Müller Research Group
New principle for the self-assembly of patterned nanoparticles published in NATURE may have important implications for nanotechnology and future technologies

Animal and plant cells are prominent examples of how nature constructs ever-larger units in a targeted, preprogrammed manner using molecules as building blocks. In nanotechnology, scientists mimic this ‘bottom-up’ technique by using the ability of suitably structured nano materials to ‘self-assemble’ into higher order architectures. Applying this concept, polymer scientists from Bayreuth, Aachen, Jena, Mainz, and Helsinki have recently published an article in the prestigious journal Nature that describes a new principle for the self-assembly of patterned nanoparticles. This principle may have important implications for the fundamental understanding of such processes as well as future technologies.

The research team is headed by Professor Axel Müller, who was holder of the Chair of Macromolecular Chemistry II at the University of Bayreuth until his retirement in 2012; he is now a Fellow of the Gutenberg Research College at Mainz University. The other members of the team are Dr. André Gröschel (previously at the University of Bayreuth, now Aalto University Helsinki), Tina Löbling and Dr. Holger Schmalz (University of Bayreuth), Dr. Andreas Walther (Interactive Materials Research Center at Aachen University), and Junior Professor Dr. Felix Schacher (Friedrich Schiller University Jena). The research was conducted at the University of Bayreuth and funded by the German Research Foundation (DFG) within the Collaborative Research Center 840 "From Particulate Nano-Systems to Mesotechnology."

The self-assembly process described in Nature commences with chain-like macromolecules with a size in the range of 10 to 20 nanometers. In chemistry, such macromolecules are called triblock terpolymers. They are composed of three linear sections (blocks) connected to each other in sequence. They are generated using a special synthetic process, i.e., the so-called "living polymerization," and are readily available to researchers. The research team was able to guide the triblock macromolecules into soft nanoparticles with a diameter of roughly 50 nanometers. The choice of solvents played a key role in this macromolecular self-assembly process. The solvents were precisely selected and used so that the varying solubility of the three blocks and the incompatibility of the polymers with one another contributed significantly to the quality of the desired interior structure of the nanoparticles.

The scientists applied this technique to two types of triblock terpolymers. These differed with regard to the chemical properties of the middle blocks. The block sequences of the macromolecules were A-B-C and A-D-C, respectively. The first results in nanoparticles with a single bonding site and tends to form spherical clusters, while the latter creates nanoparticles with two bonding sites and thus tends to form linear superstructures. Importantly, in both cases the structure of the nanoparticles is preprogrammed by the chemical structure of the source macromolecule in the same way as the structure of a protein is determined by its amino acid sequence.

However, the process of self-assembly does not end with the nanoparticles. If the nanoparticles formed by each type of macromolecule were left to their own, spherical superstructures would result on the one hand and linear superstructures on the other. Müller's team has developed and implemented a different approach. The nanoparticles with one and two bonding sites are mixed so that they aggregate together into a completely new superstructure in a process of co-assembly. In the final superstructure, the nanoparticles originating from the A-B-C molecules and nanoparticles formed by the A-D-C molecules alternate in a precisely defined pattern.

When viewed under a transmission electron microscope, the new superstructure bears a strong resemblance to a caterpillar larva, because it also consists of a series of clearly separate, regularly ordered sections. Müller's research team has thus coined the term "caterpillar micelles" for such co-assembled superstructures.

The research findings recently published in Nature represent a breakthrough in the field of hierarchical structuring and nano-engineering as it allows creating new materials by self-assemble preprogrammed particles. This could be a game changer, because so far only top-down procedures, i.e., extracting a microstructure from a larger complex, are widely accepted structuring processes. "The limitations of this technique will become all too apparent in the near future," explained Müller. "Only rarely is it possible to generate complex structures in the nanometer range."

However, a bottom-up principle of self-assembly based on that employed in nature could well represent the best way forward. One factor that makes this particularly attractive is the large number of macromolecules, which are readily available as building blocks. They can be used to incorporate specific properties in the resultant superstructures, such as sensitivity to environmental stimuli (e.g. temperature, light, electric and magnetic fields, etc.) or give them the ability to be switched on and off at will. Possible applications include nanolithography and the delivery of drugs in which the time and site of release of active substances can be preprogrammed. Here, the similarity to the structural principles of animal and plant cells becomes apparent again, where various properties are compartmentalized into areas of limited space.

The macromolecules carrying diverse functional segments can be hundreds of times smaller than a micrometer. The superstructures that such macromolecules produce have correspondingly high resolution. "Future technologies – such as tailor-made artificial cells, transistors, or components for micro/nano-robotics – may benefit significantly from this particularly delicate structuring," explained Müller. "The research findings we published in Nature do not yet have any immediate real-world applications. Nevertheless, the better we understand bottom-up processes starting with molecules in the nanometer range and moving on to the higher hierarchical levels in the micrometer range, the more likely future technologies will be within our grasp." The caterpillar micelles are in no way the only superstructures that can be produced with the self-assembling nanoparticles. "Such soft nanoparticles can be combined with inorganic or biological nano- and microparticles to create previously unknown materials with specific functions. The number of possible combinations is practically endless," concluded Müller.

Source: http://www.uni-mainz.de/presse/16804_ENG_HTML.php

Monday, October 28, 2013

Traces of DNA exposed by twisted light

Structures that put a spin on light reveal tiny amounts of DNA with 50 times better sensitivity than the best current methods, a collaboration between the University of Michigan and Jiangnan University in China has shown.
Highly sensitive detection of DNA can help with diagnosing patients, solving crimes and identifying the origins of biological contaminants such as a pathogen in a water supply.
"It really does not matter where the target DNA is from," said Nicholas Kotov, the Joseph B. and Florence V. Cejka Professor of Chemical Engineering at U-M. "In order to detect a specific DNA, we just need to know a small portion of its sequence."
Current DNA analysis methods rely on copying segments of a strand of DNA. The process unzips the double helix and then short, lab-made 'primer' DNA strands attach to each half of the original DNA. These primers kick-start the copying process, using the unzipped DNA as a template. Targeted segments of DNA can be replicated in this way, doubling every cycle. If enough DNA is produced before copying errors become a major problem, then further analysis can show whether the sample matches a suspect, for example.
But if the primers were very selective for the suspected DNA sequence, then a match could be determined by simply detecting whether the DNA had copied or not. Studies revealed that small amounts of DNA could be observed when spherical gold nanoparticles were attached to the primers. If the DNA matched suspicions, strings of particles bound together with DNA would form in the replication process. The nanoparticle solution would change color from red to blue, due to the way the strings of particles interact with light.
"Impressive detection limits were attained for short DNAs with nanoparticles; however, not for long DNA," Kotov said.
The problem, he explained, is that if the particles are further apart than a few nanometers, or millionths of a millimeter, "they do not interact strongly and the blue color does not happen." Longer strands are needed to differentiate between species and individuals with greater accuracy.
"If the strands are too short, you could mix up the DNA of a killer with that of the friend's dog—or a signature of malignant stomach cancer with the piece of a chicken burrito," Kotov said.
He and his partner Chuanlai Xu, a professor of food science and technology at Jiangnan University in China, led an effort to see whether a more subtle optical change would hold up to longer distances.
Rather than using spherical nanoparticles, the team started with nanorods, shaped like tiny Mike and Ike candies, about 62 nanometers long and 22 nanometers in diameter. They attached the primer DNA to the sides of these.
When nanorods line up, they tend to misalign by about 10 degrees. After a few rounds of copying, the gold and DNA structures resembled twisted rope ladders. Light passing through the spiral of golden spokes reacted by rotating.
"The light can be rotated even when the nanorods are far away from each other," Kotov said. "This gives our methods a tremendous advantage in sensitivity for long DNA strands."
The rotation happens because light is composed of electric and magnetic waves moving in tandem, and electric and magnetic fields exert forces on charged particles that have freedom to move, such as electrons in metals. The electrons in gold respond very well to the frequency of visible light waves, so they begin to move back and forth in the gold, synced with the light. This effect is a two-way street: the moving electrons in the gold can also affect the light waves.
Kotov compares the light to a rope with ripples running through it.
"Now imagine that the air around the rope can move more easily along certain directions," Kotov said.
For light passing through the gold nanorods, it's easiest if the electric wave moves up and down the length of the nanorods, so the light rotates as it moves from nanorod to nanorod and continues twisting after it leaves the structure. And depending on whether the light starts out rotating clockwise or counterclockwise, it feels the twist from the nanorods most at different wavelengths.
"For analytical purposes, this is a gift," Kotov said.
The two peaks in the amount of twisting for clockwise and counterclockwise light can be added together, which makes for a stronger signal and allows the method to identify a match with smaller amounts of DNA.
"The strength of the rotation reaches maximum when the gap between nanorods is 20 nanometers, which is exactly what we need for the detection of long, selective and species-specific DNA strands," Kotov said. "The calculations presented show that we can potentially increase the sensitivity even more in the future and to even longer DNAs."
The paper, "Attomolar DNA detection with Chiral Nanorod Assemblies," will be published in Nature Communications on Oct. 28. Kotov is a professor of chemical engineering, biomedical engineering, materials science and engineering, and macromolecular science and engineering.
This work was funded by the U.S. Department of Energy and National Science Foundation, National Natural Science Foundation of China, China Ministry of Science and Technology, and grants from the Ministries of Finance and Education in Jiangsu Province, China.